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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 508710Erstellt: 27. Oktober 2026

4-Bromophenylhydrazine → 4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]aniline

https://huagongshe.com/reaction/508710

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromophenylhydrazineHCID 12158—
Edukt2-Chloro-6-fluorobenzaldehydeHCID 67847—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
Produkt4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]anilineHCID 9003365831,4%

Reaktionsschritte

To a solution of 2-chloro-6-fluorobenzaldehyde (1.0 g, 6.32 mmol) in ethanol was added (4-bromophenyl)hydrazine (1.7 g, 7.59 mmol) and aq. solution of NaHCO3 (0.637 g, 4.59 mmol). The reaction mixture was stirred at RT for 5-6 h. The reaction mass was quenched in water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated. The obtained crude product was purified by column chromatography on silica gel, eluting with 4.6% EA: pet. ether to afford 0.650 g of the desired product. 1H NMR (300 MHz, DMSO d6): δ 6.98 (d, J=7.8 Hz, 2H), 7.23-7.40 (m, 5H), 8.07 (s, 1H), 10.87 (br s, 1H). MS (m/z): 329.17 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096545B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-1f5e3475cc4e498981b286f562f98842
Quellennotizuspto-grants-2015_08